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合成蛋白开关:iFLinkC 的组合连接子工程

Synthetic protein switches: Combinatorial linker engineering with iFLinkC.

机构信息

Fachbereich Biologie, Technische Universität Darmstadt, Darmstadt, Germany; Centre for Synthetic Biology, Technische Universität Darmstadt, Darmstadt, Germany.

Fachbereich Biologie, Technische Universität Darmstadt, Darmstadt, Germany.

出版信息

Methods Enzymol. 2021;647:231-255. doi: 10.1016/bs.mie.2020.09.009. Epub 2020 Oct 17.

Abstract

Linker engineering constitutes a critical, yet frequently underestimated aspect in the construction of synthetic protein switches and sensors. Notably, systematic strategies to engineer linkers by predictive means remain largely elusive to date. This is primarily due to our insufficient understanding how the biophysical properties that underlie linker functions mediate the conformational transitions in artificially engineered protein switches and sensors. The construction of synthetic protein switches and sensors therefore heavily relies on experimental trial-and-error. Yet, methods for effectively generating linker diversity at the genetic level are scarce. Addressing this technical shortcoming, iterative functional linker cloning (iFLinkC) enables the combinatorial assembly of linker elements with functional domains from sequence verified repositories that are developed and stored in-house. The assembly process is highly scalable and given its recursive nature generates linker diversity in a combinatorial and exponential fashion based on a limited number of linker elements.

摘要

链接器工程在合成蛋白开关和传感器的构建中是一个至关重要但经常被低估的方面。值得注意的是,通过预测手段来设计链接器的系统策略至今仍然难以实现。这主要是由于我们对构成链接器功能的生物物理特性如何调节人工设计的蛋白开关和传感器中的构象转变了解不足。因此,合成蛋白开关和传感器的构建严重依赖于实验的反复尝试。然而,在遗传水平上有效产生链接多样性的方法却很少。为了解决这个技术上的缺点,迭代功能链接克隆(iFLinkC)使我们能够组合来自内部开发和存储的经过序列验证的库的功能域的链接元件。该组装过程具有高度的可扩展性,并且由于其递归性质,根据有限数量的链接元件以组合和指数的方式生成链接多样性。

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